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[高效生成苯炔的方法的开发]

[Development of Efficient Methods for Benzyne Generation].

作者信息

Takagi Akira

机构信息

Graduate School of Pharmaceutical Sciences, Osaka University.

出版信息

Yakugaku Zasshi. 2018;138(1):27-35. doi: 10.1248/yakushi.17-00157.

Abstract

2-[(Neopentyl glycolato)boryl]phenyl triflates, readily synthesized from 2-iodophenol derivatives via halogen-magnesium exchange or Miyaura borylation, were developed as new benzyne precursors. Benzynes were generated under fluoride-ion-mediated conditions and reacted immediately with various arynophiles. Herein, we describe the generation of benzynes having reactive functional groups, such as methoxycarbonyl, acetyl, bromo, and amino groups, as well as their [4+2], (3+2), and [2+2] cycloaddition reactions which produce corresponding benzo-fused compounds.

摘要

通过卤素-镁交换或宫浦硼化反应由2-碘苯酚衍生物轻松合成的2-[(新戊二醇基)硼基]苯基三氟甲磺酸酯,被开发为新型苯炔前体。苯炔在氟离子介导的条件下生成,并立即与各种亲芳炔体反应。在此,我们描述了具有反应性官能团(如甲氧基羰基、乙酰基、溴和氨基)的苯炔的生成,以及它们的[4+2]、(3+2)和[2+2]环加成反应,这些反应生成相应的苯并稠合化合物。

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